Delgado-Valverde Mercedes, Sojo-Dorado Jesús, Pascual Alvaro, Rodríguez-Baño Jesús
Infectious Diseases and Clinical Microbiology Unit, Hospital Universitario Virgen Macarena, Seville, Spain.
Infectious Diseases and Clinical Microbiology Unit, Hospital Universitario Virgen Macarena, and Department of Microbiology, University of Seville, Seville, Spain.
Ther Adv Infect Dis. 2013 Apr;1(2):49-69. doi: 10.1177/2049936113476284.
Enterobacteriaceae showing resistance to cephalosporins due to extended-spectrum β-lactamases (ESBLs) or plasmid-mediated AmpC enzymes, and those producing carbapenemases have spread worldwide during the last decades. Many of these isolates are also resistant to other first-line agents such as fluoroquinolones or aminoglycosides, leaving few available options for therapy. Thus, older drugs such as colistin and fosfomycin are being increasingly used. Infections caused by these bacteria are associated with increased morbidity and mortality compared with those caused by their susceptible counterparts. Most of the evidence supporting the present recommendations is from in vitro data, animal studies, and observational studies. While carbapenems are considered the drugs of choice for ESBL and AmpC producers, recent data suggest that certain alternatives may be suitable for some types of infections. Combined therapy seems superior to monotherapy in the treatment of invasive infections caused by carbapenemase-producing Enterobacteriaceae. Optimization of dosage according to pharmacokinetics/pharmacodynamics data is important for the treatment of infections caused by isolates with borderline minimum inhibitory concentration due to low-level resistance mechanisms. The increasing frequency and the rapid spread of multidrug resistance among the Enterobacteriaceae is a true and complex public health problem.
在过去几十年中,因产超广谱β-内酰胺酶(ESBLs)或质粒介导的AmpC酶而对头孢菌素耐药的肠杆菌科细菌,以及产碳青霉烯酶的细菌已在全球范围内传播。这些分离株中的许多还对其他一线药物如氟喹诺酮类或氨基糖苷类耐药,使得治疗选择很少。因此,黏菌素和磷霉素等较老的药物正越来越多地被使用。与由敏感菌引起的感染相比,这些细菌引起的感染与发病率和死亡率增加有关。支持目前建议的大多数证据来自体外数据、动物研究和观察性研究。虽然碳青霉烯类被认为是产ESBL和AmpC菌的首选药物,但最近的数据表明某些替代药物可能适用于某些类型的感染。在治疗由产碳青霉烯酶的肠杆菌科细菌引起的侵袭性感染时,联合治疗似乎优于单一治疗。根据药代动力学/药效学数据优化剂量对于治疗因低水平耐药机制而最低抑菌浓度处于临界值的分离株引起的感染很重要。肠杆菌科细菌中多药耐药的频率不断增加且迅速传播是一个真实而复杂的公共卫生问题。